- Integra LifeSciences (Mansfield, MA)
- …operation, disassembly, maintenance, cleaning, troubleshooting, monitoring, and programming of manufacturing equipment at the facility. + Effectively start, stop, ... required. + Lead training initiatives for new and existing operators participating in manufacturing operations. + Perform Development and Design Work + Assist in the… more
- Saint-Gobain (Bristol, RI)
- The Senior Quality Engineer will be responsible for ensuring 100% customer satisfaction by implementing effective quality methods and processes in collaboration with ... This team could include the Aerospace or Automotive markets. The Senior Quality Engineer will have ownership for understanding and implementing all market (AS-9100 /… more
- Integra LifeSciences (Mansfield, MA)
- …what's possible and making headway to help improve outcomes. The **Quality Design Engineer II ** will work within the Integra Lifesciences CSS Quality ... well as design related aspects of product and process transfers between manufacturing sites. This position will have responsibility for new product introduction and… more
- Sensata Technologies, Inc. (Attleboro, MA)
- …phase to ensure economical and defect free manufacture. Develop new or improve manufacturing and testing processes that are necessary to achieve the performance and ... site personnel. Support improvement projects to reduce cycle time, defects and manufacturing cost. Work with suppliers and contract manufacturers to ensure processes… more
- Integra LifeSciences (Mansfield, MA)
- …successful application of these techniques on a day-to-day basis in manufacturing . + Analyze/review effectiveness of preventive and corrective actions. Review root ... experience + This position will require relevant experience working in manufacturing /operations. + In-depth knowledge of product/process Risk Management (FDA and ISO… more
- Integra LifeSciences (Mansfield, MA)
- …and investigations, including failure analysis. + Review quality and manufacturing records, including DHRs, NCs, CAPAs, complaint records, failure analysis ... data and reports, and risk documentation as part of the overall complaint investigation process. + Perform trending and risk analysis of received complaint investigations; determine if upper controls have been exceeded and evaluate risk to patient. + Perform… more
- ThermoFisher Scientific (Plainville, MA)
- …Work:** At Thermo Fisher Scientific, we offer an exceptional opportunity for a Quality Engineer II to make a significant impact. As a Quality Engineer ... will include reviewing and approving validation documentation for clinical and commercial drug manufacturing of cell and gene therapy products. You will be a key… more